K-number	K072683
Device name	AXXENT ELECTRONIC BRACHYTHERAPY SYSTEM
Applicant	Xoft, Inc.
Product code	JAD
Device class	Class II
Decision date	Feb 29, 2008
Decision	Unknown
Regulation	892.5900

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View the full FDA submission: accessdata.fda.gov

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AXXENT ELECTRONIC BRACHYTHERAPY SYSTEM

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